Canonical Allele Identifier: PA2826317917
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2581394
ClinVar RCV Id: RCV003331799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.His778Leu
CA388034438
NM_001243182.2:c.2333A>T